Medical Device Recall: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Johnson & Johnson Vision Care, Inc. · June 12, 2025
Reason for Recall
Due to defects (bubbles/voids) identified during standard finished goods testing
Distribution
Worldwide - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, DE, FL, GA, HI, IA, IL, IN, KN, KS, KY, LA, MA, MD, MI, MO, NC, NJ, NV, NY, OH, PA, SC TN, TX, UT, VA, WA, WI, and WY. The countries of Belgium, Bermuda, Canada, Switzerland, Denmark, Germany, Spain, France, United Kingdom, Italy, Netherlands, Poland, Sweden, Singapore, and South Korea.
States Affected
NATIONWIDE
Quantity Affected
114,165 lenses
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2163-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.